NDC | 51009-100-47, 51009-104-47, 51009-105-47, 51009-106-47 |
Set ID | 7f20f8a0-75f9-4365-b00a-a53c6a35b448 |
Category | HUMAN OTC DRUG LABEL |
Packager | Tom's of Maine, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART355 |
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
-
Directions
adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician children 2 to 6 years use only a pea-sized amount and supervise child's brushing and rinsing (to minimize swallowing) children under 2 years ask a dentist or physician - Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL - 133 g Carton
- PRINCIPAL DISPLAY PANEL - 133 g Carton
- PRINCIPAL DISPLAY PANEL - 133 g Carton
- PRINCIPAL DISPLAY PANEL - 133 g Carton
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INGREDIENTS AND APPEARANCE
WHOLE CARE CINNAMON CLOVE
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51009-100 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium monofluorophosphate (UNII: C810JCZ56Q) (fluoride ion - UNII:Q80VPU408O) Sodium monofluorophosphate 0.0076 g in 1 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Water (UNII: 059QF0KO0R) Calcium carbonate (UNII: H0G9379FGK) Hydrated Silica (UNII: Y6O7T4G8P9) Xylitol (UNII: VCQ006KQ1E) Carrageenan (UNII: 5C69YCD2YJ) Zinc citrate (UNII: K72I3DEX9B) Sodium Lauryl Sulfate (UNII: 368GB5141J) Cinnamon leaf oil (UNII: S92U8SQ71V) Clove oil (UNII: 578389D6D0) Clove stem oil (UNII: 9368YZM9M4) Product Characteristics Color WHITE (off-white) Score Shape Size Flavor CINNAMON (Cinnamon-Clove) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51009-100-47 1 in 1 CARTON 1 133 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 02/14/2011 WHOLE CARE PEPPERMINT
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51009-104 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium monofluorophosphate (UNII: C810JCZ56Q) (fluoride ion - UNII:Q80VPU408O) Sodium monofluorophosphate 0.0076 g in 1 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Water (UNII: 059QF0KO0R) Calcium carbonate (UNII: H0G9379FGK) Hydrated Silica (UNII: Y6O7T4G8P9) Xylitol (UNII: VCQ006KQ1E) Carrageenan (UNII: 5C69YCD2YJ) Zinc citrate (UNII: K72I3DEX9B) Sodium Lauryl Sulfate (UNII: 368GB5141J) Peppermint Oil (UNII: AV092KU4JH) Product Characteristics Color WHITE (off-white) Score Shape Size Flavor PEPPERMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51009-104-47 1 in 1 CARTON 1 133 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 02/14/2011 WHOLE CARE SPEARMINT
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51009-105 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium monofluorophosphate (UNII: C810JCZ56Q) (fluoride ion - UNII:Q80VPU408O) Sodium monofluorophosphate 0.0076 g in 1 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Water (UNII: 059QF0KO0R) Calcium carbonate (UNII: H0G9379FGK) Hydrated Silica (UNII: Y6O7T4G8P9) Xylitol (UNII: VCQ006KQ1E) Carrageenan (UNII: 5C69YCD2YJ) Zinc citrate (UNII: K72I3DEX9B) Sodium Lauryl Sulfate (UNII: 368GB5141J) Spearmint Oil (UNII: C3M81465G5) Peppermint Oil (UNII: AV092KU4JH) Product Characteristics Color WHITE (off-white) Score Shape Size Flavor SPEARMINT (Spearmint Ice) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51009-105-47 1 in 1 CARTON 1 133 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 02/14/2011 WHOLE CARE WINTERMINT
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51009-106 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium monofluorophosphate (UNII: C810JCZ56Q) (fluoride ion - UNII:Q80VPU408O) Sodium monofluorophosphate 0.0076 g in 1 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Water (UNII: 059QF0KO0R) Calcium carbonate (UNII: H0G9379FGK) Hydrated Silica (UNII: Y6O7T4G8P9) Xylitol (UNII: VCQ006KQ1E) Carrageenan (UNII: 5C69YCD2YJ) Zinc citrate (UNII: K72I3DEX9B) Sodium Lauryl Sulfate (UNII: 368GB5141J) Methyl salicylate (UNII: LAV5U5022Y) Peppermint Oil (UNII: AV092KU4JH) Product Characteristics Color WHITE (off-white) Score Shape Size Flavor MINT (Wintermint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51009-106-47 1 in 1 CARTON 1 133 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part355 02/14/2011 Labeler - Tom's of Maine, Inc. (052764354) Establishment Name Address ID/FEI Business Operations Tom's of Maine, Inc. 052764354 MANUFACTURE